Variant report

Variant	rs270051
Chromosome Location	chr6:128193774-128193775
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12194062	0.81[EUR][1000 genomes]
rs12204618	1.00[ASN][1000 genomes]
rs12213305	0.87[ASN][1000 genomes]
rs270023	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs270052	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4243492	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs451472	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6907718	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830799	chr6:128033100-128194511	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv1849854	chr6:128143774-128287313	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1024516	chr6:128184182-128298278	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128191400-128198800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:128191600-128193800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr6:128191600-128193800	Weak transcription	Fetal Thymus	thymus
4	chr6:128191600-128198600	Weak transcription	Thymus	Thymus
5	chr6:128192200-128193800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:128192600-128194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:128192800-128197200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr6:128193000-128193800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr6:128193000-128193800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr6:128193200-128195400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:128193400-128194000	Weak transcription	Primary T cells from cord blood	blood
12	chr6:128193400-128194000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr6:128193400-128194200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:128193400-128198200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links